Syntaxin 1B Protein (STX1B) (Myc-DYKDDDDK Tag)
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- Target See all Syntaxin 1B (STX1B) Proteins
- Syntaxin 1B (STX1B)
- Protein Type
- Recombinant
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Origin
- Human
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Source
- HEK-293 Cells
- Purification tag / Conjugate
- This Syntaxin 1B protein is labelled with Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Characteristics
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- Recombinant human Syntaxin 1B / STX1B protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
- Purity
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product STX1B Protein
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- Application Notes
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Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays - Comment
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The tag is located at the C-terminal.
- Restrictions
- For Research Use only
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- Concentration
- 50 μg/mL
- Buffer
- 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
- Storage
- -80 °C
- Storage Comment
- Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
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- Target
- Syntaxin 1B (STX1B)
- Alternative Name
- Syntaxin 1b,stx1b (STX1B Products)
- Synonyms
- STX1B2 Protein, STX1B Protein, stx1b1 Protein, stx1b2 Protein, STX1B1 Protein, Stx1b2 Protein, Stx1bl Protein, Syn1b Protein, Stx2 Protein, syntaxin1b Protein, wu:fb76h10 Protein, zgc:92909 Protein, syntaxin 1B Protein, syntaxin 1A Protein, syntaxin 1B L homeolog Protein, syntaxin1B Protein, STX1B Protein, STX1A Protein, stx1b Protein, LOC100136181 Protein, stx1b.L Protein, Stx1b Protein
- Background
- The protein encoded by this gene belongs to a family of proteins thought to play a role in the exocytosis of synaptic vesicles. Vesicle exocytosis releases vesicular contents and is important to various cellular functions. For instance, the secretion of transmitters from neurons plays an important role in synaptic transmission. After exocytosis, the membrane and proteins from the vesicle are retrieved from the plasma membrane through the process of endocytosis. Mutations in this gene have been identified as one cause of fever-associated epilepsy syndromes. A possible link between this gene and Parkinson's disease has also been suggested.
- Molecular Weight
- 33.1 kDa
- NCBI Accession
- NP_443106
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